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Elulookirjeldus (CV)
1.Eesnimi Rita
2.Perekonnanimi Teek
3.Töökoht SA TÜ Kliinikumi Ühendlabori Meditsiinigeneetika Keskus;
Tartu Ülikooli Arstiteaduskond
4.Ametikoht meditsiinigeneetika resident;
üldarst
5.Sünniaeg 24.10.1968 (päev.kuu.aasta)
6.Haridus Tartu Ülikool, arstiteaduskond, ravi eriala 1995
7.Teenistuskäik alates 01.2004 SA TÜK Ühendlabori Meditsiinigeneetika Keskus, üldarst;
alates 09.1999 TÜ Arstiteaduskond, meditsiinigeneetika resident;
1995-1998 Tallinna Mustamäe Haiglas internatuur;
1992-1995 Tartu Kliiniline Haigla, infarktiravi osakond, med. õde;
1991 Tartu Kliiniline Haigla, infarktiravi osakond, sanitar;
1987-1989 ENSV TM IV Valitsuse Vabariiklik Haigla, anestesioloogia-reanimatoloogia osakond, hooldusõde
8.Teaduskraad MD
9.Teaduskraadi välja
andnud asutus, aasta		 Tartu Ülikool 1995
10.Tunnustused
11.Teadusorganisatsiooniline
ja –administratiivne
tegevus		 Eesti Nooremarstide Ühenduse ja Eesti Inimesegeneetika
Ühingu liige
12.Juhendamisel kaitstud
väitekirjad
13.Teadustöö põhisuunad Kliiniline geneetika
kurtuse geneetika
14.Jooksvad grandid
15.Teaduspublikatsioonid

Teek R, Rein R, Essentson E, Marats I, Õunap K. Familial Rubinstein-Taybi syndrome. Eur J Hum Genet 2005: Vol 13, Suppl 1: 119. Thesis and poster presentation in European Human Genetics Conference 2005 in Prague.

Teek R, Õunap K, Zordania R, Zõrjanova T, Tammur P, Bartsch O. Case report: Boy with severe hypotonia, hypogenitalism, chronic interstitial pneumonia, and partial X disomy, karyotype 46,X,der(Y)t(X;Y)(q28;q11.2). Eur J Hum Genet 2004: Vol 12, Suppl 1: 129. Thesis and poster presentation in European Human Genetics Conference 2004 in Munich.

Mikelsaar RV, Teek R, Varb K, Süvari A, Pericentric inversion of 20 chromosome and mental retardation, thesis in Estonian Society of Human Genetics I Annual Conference "Genetics 2000".

viimati muudetud: 15.08.2005

Curriculum Vitae (CV)
1.First Name Rita
2.Surname Teek
3.Institution Tartu University Clinics, United Laboratories, Medical Genetics Center;
University of Tartu, Faculty of Medicine
4.Position Medical Doctor (MD);
Resident of medical genetics
5.Date of birth 24.10.1968 (day.month.year)
6.Education University of Tartu, Faculty of Medicine, Medical Doctor (MD) 1995
7.Research and
professional experience		 Since 01.2004 Tartu University Clinics, United Laboratories, Medical Genetics Center, Medical Doctor;
Since 09.1999 University of Tartu, Faculty of Medicine, Postgraduated medical training (residency) in medical genetics;
1995-1998 Tallinn Mustamäe Hospital, General medical postgraduate training (internship);
1992-1995 Tartu Clinical Hospital, Department of the Emergency Cardiology, Medical nurse;
1991 Tartu Clinical Hospital, Department of the Emergency Cardiology, Ward assistant;
1987-1989 ESSR Ministery of Healthcare IVth Government Republican Hospital, Department of the Anaesthesiology and Intensive Care, Assistant nurse
8.Academic degree MD
9.Dates and sites of
earning the degrees		 University of Tartu 1995
10.Honours/awards
11.Research-administrative
experience		 1999 Estonian Society of Human Genetics, membership;
1998 Junior Doctors' Association, membership
12.Supervised dissertations
13.Current research program Clinical genetics
Hereditary Hearing Loss and Deafness
14.Current grant funding
15.List of most important publications

Teek R, Rein R, Essentson E, Marats I, Õunap K. Familial Rubinstein-Taybi syndrome. Eur J Hum Genet 2005: Vol 13, Suppl 1: 119. Thesis and poster presentation in European Human Genetics Conference 2005 in Prague.

Teek R, Õunap K, Zordania R, Zõrjanova T, Tammur P, Bartsch O. Case report: Boy with severe hypotonia, hypogenitalism, chronic interstitial pneumonia, and partial X disomy, karyotype 46,X,der(Y)t(X;Y)(q28;q11.2). Eur J Hum Genet 2004: Vol 12, Suppl 1: 129. Thesis and poster presentation in European Human Genetics Conference 2004 in Munich.

Mikelsaar RV, Teek R, Varb K, Süvari A, Pericentric inversion of 20 chromosome and mental retardation, thesis in Estonian Society of Human Genetics I Annual Conference "Genetics 2000".

last updated: 15.08.2005

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